Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 3.2E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda
0 6 0 0 1 3.1E-03
Secondary acquired sideroblastic anemia
0 2 0 0 1 3.2E-03
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome
0 4 0 0 1 3.1E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia
0 1 0 0 1 3.2E-03
Mean corpuscular hemoglobin concentration determination
0 19 0 0 1 3.0E-03
Total iron binding capacity function
0 35 0 0 1 2.9E-03
Severe nonproliferative diabetic retinopathy
0 3 0 0 1 3.2E-03
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 3.2E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 3.2E-03
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor
0 1 0 0 1 3.2E-03
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement
0 36 0 0 1 2.9E-03
Iron binding capacity total measurement
0 35 0 0 1 2.9E-03
CORONARY ARTERY DISEASE, MODIFIER OF
0 1 0 0 1 3.2E-03
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0 1 0 0 1 3.2E-03
ALZHEIMER DISEASE, SUSCEPTIBILITY TO
0 3 0 0 1 3.2E-03
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE
0 26 0 0 1 2.9E-03
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
0 1 0 0 1 3.2E-03
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
0 1 0 0 1 3.2E-03
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
0 2 0 0 1 3.2E-03
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC
0 1 0 0 1 3.2E-03
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
0 2 0 0 1 3.2E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 3.2E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 3.2E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0 1 0 0 1 3.2E-03